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Live Birth after Fresh Embryo Transfer vs Elective Embryo Cryopreservation/Frozen Embryo Transfer in Women with Polycystic Ovary Syndrome undergoing IVF: A multi-center prospective randomized clinical trial

Live Birth after Fresh Embryo Transfer vs Elective Embryo Cryopreservation/Frozen Embryo Transfer in Women with Polycystic Ovary Syndrome undergoing IVF: A multi-center prospective randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003176
Enrollment
Unknown
Registered
2013-04-17
Start date
2013-06-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

polycystic ovary syndrome

Interventions

fresh embryo transfer group:rFSH/GnRH antagonist ovarian hyperstimulation, oocyte pick-up, fresh embryo transfer, luteal phase support, follow-up
frozen-thawed embryo transfer group:rFSH/GnRH antagonist ovarian hyperstimulation, oocyte pick-up, all embryos cryopreservation, frozen-thawed embryo transfer, luteal phase support, follow-up

Sponsors

Reproductive medical Hospital affiliated to Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 34 Years

Inclusion criteria

Inclusion criteria: 1. Women diagnosed as PCOS according to Chinese PCOS diagnosis criteria; 2. Women who have >=1 years history of infertility; 3. Women aged >=20 and 3; 8. Women who are capable of giving informed consent.

Exclusion criteria

Exclusion criteria: 1. Women who underwent unilateral ovariectomy; 2. Women diagnosed as uterus abnormality: malformed uterus (uterus unicornis, septate uterus, duplex uterus, uterus bicomis), adenomyosis, submucous myoma, intrauterine adhesion; 3. Women or their partner with abnormal chromosome karyotype including chromosome polymorphism; 4. Women who have experienced recurrent spontaneous abortion (including biochemical pregnancy abortion) more than 2 times; 5. Women with medical condition that represent contraindication to assisted reproductive technology and/or pregnancy, such as poorly controlled Type I or Type II diabetes; undiagnosed liver disease or dysfunction (based on serum liver enzyme testing); renal disease or abnormal serum renal function; significant anemia; history of deep venous thrombosis, pulmonary embolus, or cerebrovascular accident; uncontrolled hypertension, known symptomatic heart disease; history of or suspected cervical carcinoma, endometrial carcinoma, or breast carcinoma; undiagnosed vaginal bleeding; 6. Women who has developed severe OHSS before oocyte pick-up day; 7. Women with retrieved oocytes number <=3; 8. Women who are unable to comply with the study procedures.

Design outcomes

Primary

MeasureTime frame
live birth rate;

Secondary

MeasureTime frame
OHSS incidence;clinical pregnancy rate;pregnancy loss rate;ectopic pregnancy rate;singleton live birth rate;pregnancy complication incidence;Congenital Anomalies rate;Neonatal complication rate;

Countries

China

Contacts

Public ContactZi-jiang Chen
chenzijiang59@gmail.com+86 0531 85651190

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026